raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:108997

Rare anemia

Type
Category
Group
Group of disorders
Status
active

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare anemia
frAnémie rare
deAnämie, seltene
esAnemia rara
itAnemia rara
nlZeldzame anemie
ptAnemia rara
plRzadka niedokrwistość
csVzácné anémie
ukРідкісна анемія
zh罕见贫血
trNadir anemi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15223Evalidated
UMLSC5681755Evalidated
GARD19869Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

Children (6):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card